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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50055Generated: October 26, 2026

Water → 1-(Benzyloxycarbonyl)-4-phenylpiperidine-4-carboxylic acid

https://huagongshe.com/reaction/50055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
Reactant4-Piperidinecarboxylic acid, 4-phenyl-, 4-methylbenzenesulfonate (1:1)HCID 2723657—
SolventAcetoneHCID 180—
Product1-(Benzyloxycarbonyl)-4-phenylpiperidine-4-carboxylic acidHCID 2274179890.3%

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of 37.7 g of 4-carboxy-4-phenylpiperidine p-toluenesulfonate, 53.3 g of 30% aqueous NaOH solution and 250 ml of water is cooled to 5° C. A solution of 18 g of benzyl chloroformate in 60 ml of acetone is added rapidly at 5° C. and the reaction mixture is stirred overnight, the temperature being allowed to rise to RT. It is washed twice with ether and, after decantation, the aqueous phase is acidified to pH 1 by the addition of concentrated HCl and then 2 N HCl. The precipitate formed is filtered off, dried, taken up with ether and filtered off again to give 30.6 g of the expected product, m.p.=142-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710042B2
Source datasetuspto-grants-2004_03
ORD IDord-bc0f94f9e9c1453c86a8f5411fc78675
Source noteuspto-grants-2004_03